Canonical Allele Identifier: PA2828545959
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361663.1:p.Leu7640Phe
CA139164585
NM_001374734.1:c.22918C>T